PD-L1 expression by Tumor Proportion Score (TPS) and Combined Positive Score (CPS) are similar in non-small cell lung cancer (NSCLC)
BackgroundFor non-small cell lung cancer (NSCLC) the most used method for analysing programmed cell death ligand 1 (PD-L1) expression is the Tumor Proportion Score (TPS). Nevertheless, for other tumour types, the Combined Positive Score (CPS) has been the method of choice.AimEvaluate and compare the...
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Veröffentlicht in: | Journal of clinical pathology 2021-11, Vol.74 (11), p.735-740 |
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description | BackgroundFor non-small cell lung cancer (NSCLC) the most used method for analysing programmed cell death ligand 1 (PD-L1) expression is the Tumor Proportion Score (TPS). Nevertheless, for other tumour types, the Combined Positive Score (CPS) has been the method of choice.AimEvaluate and compare the predictive value of both CPS and TPS as predictors of immunotherapy response in NSCLC, and to evaluate the agreement intra-observer between both methods and inter-observer between two expert lung pathologists.Methods56 NSCLC patients who were treated with anti-programmed cell death 1 (PD-1)/PD-L1 therapy were included. Two pathologists evaluated all cases independently, considering the sample’s adequacy for analysis, and the PD-L1 expression by TPS and CPS.ResultsThe Kappa coefficient for adequacy was 0.82 (95% CI 0.67 to 0.97). There was a high agreement between TPS and CPS and a high agreement between pathologists concerning the two methods. The Kappa coefficient between TPS and CPS was 0.85 for both pathologists, and between pathologists was 0.94 and 0.93 for TPS and CPS, respectively.ConclusionsBoth methods proved to be equally predictive of response to anti-PD-1/PD-L1 therapy. There was both a high intra-observer agreement between the two methods and a high inter-observer agreement between pathologists. This study suggests that CPS could also be used in a routine setting for immunotherapy decision in NSCLC. |
doi_str_mv | 10.1136/jclinpath-2020-206832 |
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Nevertheless, for other tumour types, the Combined Positive Score (CPS) has been the method of choice.AimEvaluate and compare the predictive value of both CPS and TPS as predictors of immunotherapy response in NSCLC, and to evaluate the agreement intra-observer between both methods and inter-observer between two expert lung pathologists.Methods56 NSCLC patients who were treated with anti-programmed cell death 1 (PD-1)/PD-L1 therapy were included. Two pathologists evaluated all cases independently, considering the sample’s adequacy for analysis, and the PD-L1 expression by TPS and CPS.ResultsThe Kappa coefficient for adequacy was 0.82 (95% CI 0.67 to 0.97). There was a high agreement between TPS and CPS and a high agreement between pathologists concerning the two methods. The Kappa coefficient between TPS and CPS was 0.85 for both pathologists, and between pathologists was 0.94 and 0.93 for TPS and CPS, respectively.ConclusionsBoth methods proved to be equally predictive of response to anti-PD-1/PD-L1 therapy. There was both a high intra-observer agreement between the two methods and a high inter-observer agreement between pathologists. This study suggests that CPS could also be used in a routine setting for immunotherapy decision in NSCLC.</description><identifier>ISSN: 0021-9746</identifier><identifier>EISSN: 1472-4146</identifier><identifier>DOI: 10.1136/jclinpath-2020-206832</identifier><identifier>PMID: 33589532</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Association of Clinical Pathologists</publisher><subject>Apoptosis ; Biomarkers ; Cancer therapies ; Chemotherapy ; Histology ; immunohistochemistry ; Immunotherapy ; Ligands ; Lung cancer ; lung neoplasms ; Metastasis ; Oncology ; Original research ; Response rates ; Sample size ; Survival analysis ; tumour</subject><ispartof>Journal of clinical pathology, 2021-11, Vol.74 (11), p.735-740</ispartof><rights>Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><rights>2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b472t-31bda23de6e89e3a27c180593c99226c55e9c5922fd71f31cbcbfa8a19659c563</citedby><cites>FETCH-LOGICAL-b472t-31bda23de6e89e3a27c180593c99226c55e9c5922fd71f31cbcbfa8a19659c563</cites><orcidid>0000-0001-5259-0215</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33589532$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>De Marchi, Pedro</creatorcontrib><creatorcontrib>Leal, Leticia Ferro</creatorcontrib><creatorcontrib>Duval da Silva, Vinicius</creatorcontrib><creatorcontrib>da Silva, Eduardo Caetano Albino</creatorcontrib><creatorcontrib>Cordeiro de Lima, Vladmir Claudio</creatorcontrib><creatorcontrib>Reis, Rui Manuel</creatorcontrib><title>PD-L1 expression by Tumor Proportion Score (TPS) and Combined Positive Score (CPS) are similar in non-small cell lung cancer (NSCLC)</title><title>Journal of clinical pathology</title><addtitle>J Clin Pathol</addtitle><addtitle>J Clin Pathol</addtitle><description>BackgroundFor non-small cell lung cancer (NSCLC) the most used method for analysing programmed cell death ligand 1 (PD-L1) expression is the Tumor Proportion Score (TPS). Nevertheless, for other tumour types, the Combined Positive Score (CPS) has been the method of choice.AimEvaluate and compare the predictive value of both CPS and TPS as predictors of immunotherapy response in NSCLC, and to evaluate the agreement intra-observer between both methods and inter-observer between two expert lung pathologists.Methods56 NSCLC patients who were treated with anti-programmed cell death 1 (PD-1)/PD-L1 therapy were included. Two pathologists evaluated all cases independently, considering the sample’s adequacy for analysis, and the PD-L1 expression by TPS and CPS.ResultsThe Kappa coefficient for adequacy was 0.82 (95% CI 0.67 to 0.97). There was a high agreement between TPS and CPS and a high agreement between pathologists concerning the two methods. The Kappa coefficient between TPS and CPS was 0.85 for both pathologists, and between pathologists was 0.94 and 0.93 for TPS and CPS, respectively.ConclusionsBoth methods proved to be equally predictive of response to anti-PD-1/PD-L1 therapy. There was both a high intra-observer agreement between the two methods and a high inter-observer agreement between pathologists. This study suggests that CPS could also be used in a routine setting for immunotherapy decision in NSCLC.</description><subject>Apoptosis</subject><subject>Biomarkers</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Histology</subject><subject>immunohistochemistry</subject><subject>Immunotherapy</subject><subject>Ligands</subject><subject>Lung cancer</subject><subject>lung neoplasms</subject><subject>Metastasis</subject><subject>Oncology</subject><subject>Original research</subject><subject>Response rates</subject><subject>Sample size</subject><subject>Survival analysis</subject><subject>tumour</subject><issn>0021-9746</issn><issn>1472-4146</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkUFv1DAUhC0EotvCT6CyxGV7CPjZcRIfq0AL0gpW2uVsOY4DXiV2aieI3vvD6-22i9QD4vL8ZH8zGmsQegfkAwArPu50b92opl8ZJZSkUVSMvkALyEua5ZAXL9GCEAqZKPPiBJ3GuCMEWAnsNTphjFeCM7pAd-tP2Qqw-TMGE6P1Dje3eDsPPuB18KMP0_5uo30weLldby6wci2u_dBYZ1q89tFO9rd5IuoHIm3RDrZXAVuHnXdZHFTfY23S6Gf3E2vltAl4-W1Tr-qLN-hVp_po3j6eZ-jH1edt_SVbfb_-Wl-usiZ9asoYNK2irDWFqYRhipYaKsIF00JQWmjOjdA8rV1bQsdAN7rpVKVAFDw9FOwMLQ--Y_A3s4mTHGzch1LO-DlKmgsCIASUCX3_DN35ObiUTlJeMQZlXuaJ4gdKBx9jMJ0cgx1UuJVA5L4meaxJ7muSh5qS7vzRfW4G0x5VT70kgByAZtj9tyf8lRzD_ltzD9ASrXc</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>De Marchi, Pedro</creator><creator>Leal, Leticia Ferro</creator><creator>Duval da Silva, Vinicius</creator><creator>da Silva, Eduardo Caetano Albino</creator><creator>Cordeiro de Lima, Vladmir Claudio</creator><creator>Reis, Rui Manuel</creator><general>BMJ Publishing Group Ltd and Association of Clinical Pathologists</general><general>BMJ Publishing Group LTD</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BTHHO</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-5259-0215</orcidid></search><sort><creationdate>20211101</creationdate><title>PD-L1 expression by Tumor Proportion Score (TPS) and Combined Positive Score (CPS) are similar in non-small cell lung cancer (NSCLC)</title><author>De Marchi, Pedro ; Leal, Leticia Ferro ; Duval da Silva, Vinicius ; da Silva, Eduardo Caetano Albino ; Cordeiro de Lima, Vladmir Claudio ; Reis, Rui Manuel</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b472t-31bda23de6e89e3a27c180593c99226c55e9c5922fd71f31cbcbfa8a19659c563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Apoptosis</topic><topic>Biomarkers</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Histology</topic><topic>immunohistochemistry</topic><topic>Immunotherapy</topic><topic>Ligands</topic><topic>Lung cancer</topic><topic>lung neoplasms</topic><topic>Metastasis</topic><topic>Oncology</topic><topic>Original research</topic><topic>Response rates</topic><topic>Sample size</topic><topic>Survival analysis</topic><topic>tumour</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>De Marchi, Pedro</creatorcontrib><creatorcontrib>Leal, Leticia Ferro</creatorcontrib><creatorcontrib>Duval da Silva, Vinicius</creatorcontrib><creatorcontrib>da Silva, Eduardo Caetano Albino</creatorcontrib><creatorcontrib>Cordeiro de Lima, Vladmir Claudio</creatorcontrib><creatorcontrib>Reis, Rui Manuel</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>De Marchi, Pedro</au><au>Leal, Leticia Ferro</au><au>Duval da Silva, Vinicius</au><au>da Silva, Eduardo Caetano Albino</au><au>Cordeiro de Lima, Vladmir Claudio</au><au>Reis, Rui Manuel</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PD-L1 expression by Tumor Proportion Score (TPS) and Combined Positive Score (CPS) are similar in non-small cell lung cancer (NSCLC)</atitle><jtitle>Journal of clinical pathology</jtitle><stitle>J Clin Pathol</stitle><addtitle>J Clin Pathol</addtitle><date>2021-11-01</date><risdate>2021</risdate><volume>74</volume><issue>11</issue><spage>735</spage><epage>740</epage><pages>735-740</pages><issn>0021-9746</issn><eissn>1472-4146</eissn><abstract>BackgroundFor non-small cell lung cancer (NSCLC) the most used method for analysing programmed cell death ligand 1 (PD-L1) expression is the Tumor Proportion Score (TPS). Nevertheless, for other tumour types, the Combined Positive Score (CPS) has been the method of choice.AimEvaluate and compare the predictive value of both CPS and TPS as predictors of immunotherapy response in NSCLC, and to evaluate the agreement intra-observer between both methods and inter-observer between two expert lung pathologists.Methods56 NSCLC patients who were treated with anti-programmed cell death 1 (PD-1)/PD-L1 therapy were included. Two pathologists evaluated all cases independently, considering the sample’s adequacy for analysis, and the PD-L1 expression by TPS and CPS.ResultsThe Kappa coefficient for adequacy was 0.82 (95% CI 0.67 to 0.97). There was a high agreement between TPS and CPS and a high agreement between pathologists concerning the two methods. The Kappa coefficient between TPS and CPS was 0.85 for both pathologists, and between pathologists was 0.94 and 0.93 for TPS and CPS, respectively.ConclusionsBoth methods proved to be equally predictive of response to anti-PD-1/PD-L1 therapy. There was both a high intra-observer agreement between the two methods and a high inter-observer agreement between pathologists. This study suggests that CPS could also be used in a routine setting for immunotherapy decision in NSCLC.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and Association of Clinical Pathologists</pub><pmid>33589532</pmid><doi>10.1136/jclinpath-2020-206832</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-5259-0215</orcidid></addata></record> |
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subjects | Apoptosis Biomarkers Cancer therapies Chemotherapy Histology immunohistochemistry Immunotherapy Ligands Lung cancer lung neoplasms Metastasis Oncology Original research Response rates Sample size Survival analysis tumour |
title | PD-L1 expression by Tumor Proportion Score (TPS) and Combined Positive Score (CPS) are similar in non-small cell lung cancer (NSCLC) |
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